Concepedia

Author

Michel Michaelides

University College LondonORCID

Also Known As

Alison Hardcastle, Andrew Lotery, Andrew Mumford, Andrew R Webster, Anthony Moore, Drewry, David H., Graham E. Holder, Karyn Megy, Leema Robert, M MICHAELIDES

821

Publications

24.7K

Citations

77

H-Index

134

Concepts

All Affiliations

University College LondonMoorfields Eye HospitalMoorfields Eye Hospital NHS Foundation TrustUniversity of California, San FranciscoMedical College of Wisconsin
MM

About

Michel Michaelides is an author at University College London specializing in medicine, ophthalmology, and genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

41

78

6.1K

2

Engineering

5

5

159

3

Health Sciences

2

2

29

4

Natural Sciences

2

2

271

5

Education

1

1

122

Michel Michaelides

×

298

Publications

17.1K

Citations

68

H-Index

YearCitations

Long-Term Effect of Gene Therapy on Leber’s Congenital Amaurosis

James Bainbridge, Manjit Mehat, Venki Sundaram,

New England Journal of Medicine

2015

713

A comparison of the causes of blindness certifications in England and Wales in working age adults (16–64 years), 1999–2000 with 2009–2010

Gerald Liew, Michel Michaelides, Catey Bunce

BMJ Open

2014

641

A Prospective Randomized Trial of Intravitreal Bevacizumab or Laser Therapy in the Management of Diabetic Macular Edema (BOLT Study)

Michel Michaelides, Andrew Kaines, Robin Hamilton,

Ophthalmology

2010

506

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

Keren Carss, Gavin Arno, Marie Erwood,

The American Journal of Human Genetics

2016

463

A 2-Year Prospective Randomized Controlled Trial of Intravitreal Bevacizumab or Laser Therapy (BOLT) in the Management of Diabetic Macular Edema

Ranjan Rajendram, Samantha Fraser‐Bell, Andrew Kaines,

Archives of Ophthalmology

2012

386

Transplantation of Human Embryonic Stem Cell-Derived Retinal Pigment Epithelial Cells in Macular Degeneration

Manjit Mehat, Venki Sundaram, Caterina Ripamonti,

Ophthalmology

2018

277

Mutant prominin 1 found in patients with macular degeneration disrupts photoreceptor disk morphogenesis in mice

Zhenglin Yang, Yali Chen, Concepción Lillo,

Journal of Clinical Investigation

2008

271

Genetic Basis of Inherited Retinal Disease in a Molecularly Characterized Cohort of More Than 3000 Families from the United Kingdom

Nikolas Pontikos, Gavin Arno, Neringa Jurkutė,

Ophthalmology

2020

244

Acute retinal necrosis: a national population-based study to assess the incidence, methods of diagnosis, treatment strategies and outcomes in the UK

Manickam Nick Muthiah, Michel Michaelides, Christoper S. Child,

British Journal of Ophthalmology

2007

226

Mutations in the unfolded protein response regulator ATF6 cause the cone dysfunction disorder achromatopsia

Susanne Kohl, Ditta Zobor, Wei‐Chieh Chiang,

Nature Genetics

2015

211

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